Exploring the causal relationship: bidirectional mendelian randomization study on benign prostatic hyperplasia and cardiovascular diseases

被引:1
|
作者
Xiang, Nanyan [1 ]
Su, Shiqi [1 ]
Wang, Zeng [2 ]
Yang, Yong [3 ]
Chen, Boxi [4 ]
Shi, Rui [2 ]
Zheng, Tao [2 ]
Liao, Banghua [5 ]
Lin, Yifei [6 ,7 ]
Huang, Jin [6 ]
机构
[1] Sichuan Univ, West China Hosp, Innovat Inst Integrat Med & Engn, Frontiers Sci Ctr Dis,Ctr Dis Related Mol Network, Chengdu, Sichuan, Peoples R China
[2] Sichuan Univ, West China Hosp, Minist Educ, Engn Res Ctr Med Informat Technol, Chengdu, Sichuan, Peoples R China
[3] Sichuan Univ, West China Hosp, Innovat Inst Integrat Med & Engn, Hlth Management Ctr,Gen Practice Med Ctr, Chengdu, Sichuan, Peoples R China
[4] Sichuan Univ, West China Sch Publ Hlth, Chengdu, Sichuan, Peoples R China
[5] West China Hosp, Dept Urol, Chengdu, Sichuan, Peoples R China
[6] West China Hosp, Innovat Inst Integrat Med & Engn, Dept Urol, Chengdu, Sichuan, Peoples R China
[7] Harvard TH Chan Sch Publ Hlth, Program Genet Epidemiol & Stat Genet, Boston, MA 02115 USA
基金
中国国家自然科学基金;
关键词
benign prostatic hyperplasia; cardiovascular diseases; mendelian randomization; genetic epidemiology; causal relationship; URINARY-TRACT SYMPTOMS; RISK-FACTORS; EPIDEMIOLOGY;
D O I
10.3389/fgene.2024.1432055
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Background Benign prostatic hyperplasia (BPH) is a common disease occurring in elderly and middle-aged men, and cardiovascular diseases (CVDs) are one of the major causes of death worldwide. Many observational studies examined have found a strong association between BPH and CVDs, but the causal relationship between them is unclear. The aim of this study was to determine the causal relationship between BPH and CVDs, specifically five diseases: stroke, coronary heart disease (CHD), heart failure, myocardial infarction (MI), and atrial fibrillation (AF).Methods In this study, we obtained single nucleotide polymorphisms (SNPs) of patients with BPH from the UK Biobank database and patients with CVDs from the UK Biobank, the HERMES Consortium, and the FinnGen Genome Database, each used as a genetic tool for a Mendelian randomization (MR) study. We used conventional MR analysis to assess potential causal direction between BPH and CVDs, as well as MR-Egger, MR-PRESSO, model-based estimation (MBE) and weighted median methods for sensitivity analysis.Results Using a bidirectional two-sample MR study, we found that BPH patients had an increased risk of developing CHD (ConMix OR = 1.152, 95% CI: 1.011-1.235, p = 0.035) and MI (ConMix OR = 1.107.95% CI: 1.022-1.164, p = 0.013), but a decreased risk of stroke (ConMix OR = 0.872, 95% CI: 0.797-0.926, p = 0.002). The reverse study was not statistically significant and further research may be needed.Conclusion Our study suggests a potential causal relationship between BPH and CVDs. BPH appears to be a risk factor for CHD and MI, but it may be protective against stroke. There was no evidence of a causal association in the reverse study, and a larger sample size was needed in follow-up to further explore the potential association.
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页数:8
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